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CRC Job at Thermo Fisher Scientific | Apply for a Clinical Trial Coordinator Role Opening in UK

CRC Job at Thermo Fisher Scientific | Apply Now

CRC job opportunities in the UK are growing rapidly, especially in the clinical research and life sciences sector. Thermo Fisher Scientific is currently hiring for a Clinical Trial Coordinator position in Cambridge, United Kingdom. This life sciences job is ideal for candidates with a background in Life Sciences who are looking to begin or advance their clinical research careers. The role offers hands-on exposure to global clinical trials, regulatory processes, study coordination, and clinical operations within one of the world’s leading scientific organizations.

  • Job Position: Clinical Trial Coordinator
  • Company: Thermo Fisher Scientific
  • Category: Clinical Research
  • Location: Cambridge, United Kingdom
  • Job ID: R-01348796

About the Company

CRC job seekers looking for global clinical research opportunities can explore exciting roles at Thermo Fisher Scientific. The company is a global leader in scientific research, healthcare innovation, laboratory services, and clinical development solutions. Through its PPD® clinical research services division, Thermo Fisher Scientific supports clinical trials across more than 100 countries.

The organization focuses on enabling customers to make the world healthier, cleaner, and safer. With over 100,000 employees worldwide, the company is known for innovation, integrity, collaboration, and career growth opportunities in the life sciences sector.

CRC Job Description

CRC job responsibilities at Thermo Fisher Scientific involve providing administrative and technical support to the Project Team within clinical research operations. The selected candidate will support audit readiness activities and ensure that clinical trial documentation is reviewed according to organizational procedures and department guidance.

This life sciences job is particularly suitable for candidates interested in becoming Clinical Research Associates (CRA) in the future. The role provides foundational experience in study coordination, regulatory documentation, project tracking, and clinical trial systems. The position also includes exposure to digital and decentralized clinical trial services, supporting research programs that contribute to improved global healthcare outcomes.

Qualifications and Eligibility

CRC job applicants should meet the following educational and professional requirements:

Educational Qualification

Experience

  • 0 to 1 year of relevant experience in clinical research or related fields

Required Skills

CRC job candidates should possess the following skills and competencies:

  • Strong organizational and multitasking abilities
  • Attention to detail and accuracy
  • Ability to work independently and in teams
  • Strong communication and interpersonal skills
  • Knowledge of ICH Good Clinical Practices (GCP)
  • Understanding of country regulations and SOPs
  • Advanced MS Office proficiency
  • Ability to learn and manage clinical trial database systems
  • Strong customer-focused approach
  • Flexibility to manage changing project timelines
  • Good English communication and grammar skills

This life sciences job also requires candidates to successfully complete PPD clinical training programs.

Key Responsibilities – CRC Job

CRC job duties include:

  • Performing department, internal, country, and investigator file reviews
  • Documenting findings in appropriate systems
  • Supporting study-specific documentation and tracking systems
  • Managing project training requirements and system access tracking
  • Providing support for systems such as Activate and eTMF
  • Processing clinical trial documents and maintaining trial master files
  • Supporting internal and client meeting schedules
  • Reviewing and tracking local regulatory documentation
  • Transmitting documents to clients and IRB/IEC teams
  • Analyzing study metrics and findings reports
  • Maintaining vendor trackers and study-related records
  • Assisting with Investigator Site File (ISF) and Pharmacy binder coordination
  • Supporting translation materials and translation quality checks

This Thermo Fisher jobs opportunity provides hands-on clinical operations experience that can strengthen long-term careers in research and healthcare.

Why Join Thermo Fisher Scientific?

CRC job opportunities at Thermo Fisher Scientific provide employees with access to professional development programs, global exposure, and collaborative work environments. Employees benefit from:

  • Competitive salary packages
  • Flexible work culture
  • Learning and development programs
  • Career growth opportunities in clinical research
  • Collaborative global teams
  • Strong work-life balance initiatives

The company promotes diversity, innovation, and inclusion while supporting employees in achieving long-term career goals.

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